[({[(2S,3R,4S,5S)-5-(2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphinic acid (BioDeep_00001029198)
代谢物信息卡片
化学式: C15H24N2O17P2 (566.0550194)
中文名称:
谱图信息:
最多检出来源 () 0%
分子结构信息
SMILES: C1=CN(C(=O)NC1=O)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OC3C(C(C(C(O3)CO)O)O)O)O)O
InChI: InChI=1S/C15H24N2O17P2/c18-3-5-8(20)10(22)12(24)14(32-5)33-36(28,29)34-35(26,27)30-4-6-9(21)11(23)13(31-6)17-2-1-7(19)16-15(17)25/h1-2,5-6,8-14,18,20-24H,3-4H2,(H,26,27)(H,28,29)(H,16,19,25)/t5-,6-,8-,9-,10+,11-,12-,13-,14?/m0/s1
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相关代谢途径
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代谢反应
95 个相关的代谢反应过程信息。
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PathBank(95)
- Starch and Sucrose Metabolism:
D-Glucose + [PTS enzyme I]-N -phospho-L-histidine ⟶ -D-glucose 1-phosphate + [PTS enzyme I]-L-histidine
- Trehalose Biosynthesis I:
Glucose 6-phosphate + Uridine diphosphate glucose ⟶ , -Trehalose 6-phosphate + Hydrogen Ion + Uridine 5'-diphosphate
- Starch and Sucrose Metabolism:
Adenosine triphosphate + D-Glucose ⟶ Adenosine diphosphate + Glucose 6-phosphate
- Starch and Sucrose Metabolism:
-D-Glucose + Unknown ⟶ -D-Glucose 6-phosphate + Unknown
- Trehalose Biosynthesis I:
Glucose 6-phosphate + Uridine diphosphate glucose ⟶ , -Trehalose 6-phosphate + Hydrogen Ion + Uridine 5'-diphosphate
- Colanic Acid Building Blocks Biosynthesis:
-D-Glucose + Phosphocarrier protein HPr ⟶ -D-Glucose 6-phosphate + Phosphocarrier protein HPr
- Flavone and Flavonol Biosynthesis:
Phosphoadenosine phosphosulfate + Quercetin ⟶ Adenosine 3',5'-diphosphate + Hydrogen Ion + Quercetin 3'-sulfate
- Sphingolipid Metabolism:
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- Gaucher Disease:
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- Globoid Cell Leukodystrophy:
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- Metachromatic Leukodystrophy (MLD):
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- Fabry Disease:
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- Krabbe Disease:
Glucosylceramide (d18:1/18:0) + Water ⟶ Ceramide (d18:1/18:0) + D-Glucose
- N-Glycan Biosynthesis:
Dolichol phosphate + Uridine diphosphate-N-acetylglucosamine ⟶ N-acetyl- -D-glucosaminyl-diphosphodolichol + Uridine 5'-monophosphate
- Galactose Metabolism:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Galactosemia:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Galactosemia II (GALK):
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactosemia III:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Congenital Disorder of Glycosylation CDG-IId:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- GLUT-1 Deficiency Syndrome:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Galactose Metabolism:
-D-Glucose + Phosphocarrier protein HPr ⟶ -D-Glucose 6-phosphate + Phosphocarrier protein HPr
- Galactose Degradation/Leloir Pathway:
-D-Glucose + Phosphocarrier protein HPr ⟶ -D-Glucose 6-phosphate + Phosphocarrier protein HPr
- Leloir Pathway:
-D-Galactose ⟶ D-Galactose
- Amino Sugar and Nucleotide Sugar Metabolism:
-D-Glucose + Adenosine triphosphate ⟶ -D-Glucose 6-phosphate + Adenosine diphosphate
- Galactose Metabolism:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactosemia:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Galactosemia II (GALK):
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactosemia III:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Congenital Disorder of Glycosylation CDG-IId:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- GLUT-1 Deficiency Syndrome:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactose Metabolism:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactose Metabolism:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Nucleotide Sugars Metabolism:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Lactose Synthesis:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Galactosemia:
D-Galactose + D-Mannose ⟶ Epimelibiose
- Galactosemia II (GALK):
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Galactosemia III:
Adenosine triphosphate + D-Galactose ⟶ Adenosine diphosphate + Galactose 1-phosphate
- Congenital Disorder of Glycosylation CDG-IId:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- GLUT-1 Deficiency Syndrome:
Glucose 1-phosphate + Water ⟶ D-Glucose + Phosphate
- Abscisic Acid Glucose Ester Metabolism:
Water + abscisic acid glucose ester ⟶ (S)-Abscisic acid + D-glucopyranose + Hydrogen Ion
- Sphingolipid Metabolism:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Gaucher Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Globoid Cell Leukodystrophy:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Metachromatic Leukodystrophy (MLD):
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Fabry Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Krabbe Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Sphingolipid Metabolism:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Sphingolipid Metabolism:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Sphingolipid Metabolism:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Sphingolipid Metabolism:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Gaucher Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Globoid Cell Leukodystrophy:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Metachromatic Leukodystrophy (MLD):
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Fabry Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- Krabbe Disease:
Galactosylceramide (d18:1/16:0) + Phosphoadenosine phosphosulfate ⟶ 3-O-Sulfogalactosylceramide (d18:1/24:0) + Adenosine 3',5'-diphosphate
- cis-Zeatin-O-Glucoside Biosynthesis:
Water + cis-zeatin riboside ⟶ Cis-zeatin + D-ribofuranose
- cis-Zeatin-N-Glucoside Biosynthesis:
Water + cis-zeatin riboside ⟶ Cis-zeatin + D-ribofuranose
- Phenolic Malonylglucosides Biosynthesis:
2-Naphthol + Uridine diphosphate glucose ⟶ 2-naphthol glucoside + Hydrogen Ion + Uridine 5'-diphosphate
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Tryptophan Metabolism:
Phosphoadenosine phosphosulfate + indolylmethyl-desulfoglucosinolate ⟶ Adenosine 3',5'-diphosphate + Glucobrassicin + Hydrogen Ion
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Starch and Sucrose Metabolism:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogen Synthetase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type III. Cori Disease, Debrancher Glycogenosis:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type IV. Amylopectinosis, Anderson Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Glycogenosis, Type VI. Hers Disease:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Mucopolysaccharidosis VII. Sly Syndrome:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Sucrase-Isomaltase Deficiency:
Isovalerylglucuronide + Water ⟶ Alcohol + D-Glucuronic acid
- Amino Sugar and Nucleotide Sugar Metabolism III:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- Amino Sugar and Nucleotide Sugar Metabolism III:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
- D-Galactose Degradation (Leloir pathway):
Beta-D-Galactose ⟶ D-Galactose
- Amino Sugar and Nucleotide Sugar Metabolism II:
N-Acetyl-D-Glucosamine 6-Phosphate + Water ⟶ Acetic acid + Glucosamine 6-phosphate
PharmGKB(0)
0 个相关的物种来源信息
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。